HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Harris Teeter, LLC, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70%

purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only-hands

Flammable.  Keep away from heat and flame.

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

Skin irritation develops

Keep out of reach of children.

If swallowed get nedical help or contact a Poison Control Center right away.

Directions

• wet hands thoroghly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

SPL UNCLASSIFIED SECTION

Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds*

This product is not manufactured or distributed by GOJO industries, Inc. distributor of Purell refreshing Gel Advanced Hand Sanitizer**

SDS-MO-15036 SDA-WI-2486 DSP-MO-28 DSP-MO-34

Proudly Distributed By: Harris Teeter, LLC

Matthews, NC 28105  1-800-432-6111 or harristeeter.com

Principal Display Panel

Harris Teeter

Advanced Hand Sanitizer

Original Scent

Kills more than 99.99% of germs*

More Effective Formula

Compare to Purell Refreshing Gel Advanced Hand Sanitizer**

8 FL OZ (236 mL)

370.000/370AB

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72036-370
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
SULISOBENZONE (UNII: 1W6L629B4K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72036-370-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/17/2014
2	NDC: 72036-370-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/17/2014
3	NDC: 72036-370-56	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/17/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/17/2014

Labeler - Harris Teeter, LLC (047279351)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(72036-370)